Effect of end group of side chains on surface properties of diblock copolymers

1990 ◽  
Vol 24 (3) ◽  
pp. 333-340 ◽  
Author(s):  
Tisato Kajiyama ◽  
Tasuo Teraya ◽  
Atsushi Takahara
2001 ◽  
Vol 3 (18) ◽  
pp. 4037-4043 ◽  
Author(s):  
Antonis Kelarakis ◽  
Shao-Min Mai ◽  
Vasiliki Havredaki ◽  
V. Mark Nace ◽  
Colin Booth

2012 ◽  
Vol 3 (8) ◽  
pp. 2148 ◽  
Author(s):  
Anne-Laure Brocas ◽  
Matthieu Gervais ◽  
Stephane Carlotti ◽  
Stergios Pispas

1973 ◽  
Vol 51 (3) ◽  
pp. 219-224 ◽  
Author(s):  
C. G. Fraser ◽  
H. J. Jennings ◽  
P. Moyna

An acidic polysaccharide has been isolated from the culture medium of T. mesenterica NRRL Y-6158. The heteropolymer contained D-xylose, D-mannose, D-glucuronic acid, and O-acetyl in the molar ratios of 7:5:1:0.7, respectively. Methylation analysis of the heteropolymer indicated that it was essentially a 1 → 3-α-linked mannopyranose backbone having approximately 80% of the backbone units substituted, thus forming a very highly branched structure. The substituents on the backbone were found to be D-glucopyranosyluronic acid end-group, β-linked to the O-2 positions of the mannopyranose units, and 2-O-β-D-linked xylopyranose side-chains, linked both to the O-2 and O-4 positions of the mannopyranose backbone. The methylation analysis suggests that these side-chains are probably two or three xylopyranose units long, although a limited variation in the length of the side-chains is a possibility.


2004 ◽  
Vol 279 (2) ◽  
pp. 364-369 ◽  
Author(s):  
Takashi Nishino ◽  
Yoshimasa Urushihara ◽  
Masashi Meguro ◽  
Katsuhiko Nakamae

Langmuir ◽  
2002 ◽  
Vol 18 (25) ◽  
pp. 9990-9995 ◽  
Author(s):  
Joshua A. Orlicki ◽  
Neil O. L. Viernes ◽  
Jeffrey S. Moore ◽  
Ibrahim Sendijarevic ◽  
Anthony J. McHugh

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